Michael R. Tallack

1.4k total citations
25 papers, 1.1k citations indexed

About

Michael R. Tallack is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Michael R. Tallack has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Genetics. Recurrent topics in Michael R. Tallack's work include Kruppel-like factors research (17 papers), Hemoglobinopathies and Related Disorders (8 papers) and Genetic Syndromes and Imprinting (6 papers). Michael R. Tallack is often cited by papers focused on Kruppel-like factors research (17 papers), Hemoglobinopathies and Related Disorders (8 papers) and Genetic Syndromes and Imprinting (6 papers). Michael R. Tallack collaborates with scholars based in Australia, United States and China. Michael R. Tallack's co-authors include Andrew C. Perkins, Janelle R. Keys, Timothy L. Bailey, Graham Magor, Lei Sun, Wai Shan Yuen, Elanor N. Wainwright, Ehsan Nourbakhsh, Sean M. Grimmond and Nicole Cloonan and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Michael R. Tallack

24 papers receiving 1.1k citations

Peers

Michael R. Tallack
Maria Rosa Lidonnici Italy
Irma Slavutsky Argentina
Elenoe C. Smith United States
Hanna T. Gazda United States
Thiébaut-Noël Willig France
Manami Maeda United States
Isabelle Lamrissi‐Garcia France
Richard A. Voit United States
Sudhir Rao United States
Minh Nguyen United States
Maria Rosa Lidonnici Italy
Michael R. Tallack
Citations per year, relative to Michael R. Tallack Michael R. Tallack (= 1×) peers Maria Rosa Lidonnici

Countries citing papers authored by Michael R. Tallack

Since Specialization
Citations

This map shows the geographic impact of Michael R. Tallack's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Michael R. Tallack with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael R. Tallack more than expected).

Fields of papers citing papers by Michael R. Tallack

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael R. Tallack. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Michael R. Tallack. The network helps show where Michael R. Tallack may publish in the future.

Co-authorship network of co-authors of Michael R. Tallack

This figure shows the co-authorship network connecting the top 25 collaborators of Michael R. Tallack. A scholar is included among the top collaborators of Michael R. Tallack based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Michael R. Tallack. Michael R. Tallack is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Huang, Stephen, Casie Reed, Graham Magor, et al.. (2024). Mutations in linker-2 of KLF1 impair expression of membrane transporters and cytoskeletal proteins causing hemolysis. Nature Communications. 15(1). 7019–7019. 1 indexed citations
3.
Barbier, Valérie, Johanna Erbani, Corrine E. Fiveash, et al.. (2020). Endothelial E-selectin inhibition improves acute myeloid leukaemia therapy by disrupting vascular niche-mediated chemoresistance. Nature Communications. 11(1). 2042–2042. 120 indexed citations
4.
Gillinder, Kevin R., Danitza Nébor, Ravi Sachidanandam, et al.. (2016). Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability. Nucleic Acids Research. 45(3). 1130–1143. 34 indexed citations
5.
Bell, Charles C., Paulo Amaral, Anton M.F. Kalsbeek, et al.. (2016). The Evx1/Evx1as gene locus regulates anterior-posterior patterning during gastrulation. Scientific Reports. 6(1). 26657–26657. 21 indexed citations
6.
Winkler, Ingrid G., Valérie Barbier, Micheal Ward, et al.. (2016). Vascular E-Selectin Protects Leukemia Cells from Chemotherapy By Directly Activating Pro-Survival NF-Kb Signalling - Therapeutic Blockade of E-Selectin Dampens NF-Kb Activation. Blood. 128(22). 2823–2823. 6 indexed citations
7.
Magor, Graham, Michael R. Tallack, Debra L. Taylor, et al.. (2016). Rapid Molecular Profiling of Myeloproliferative Neoplasms Using Targeted Exon Resequencing of 86 Genes Involved in JAK-STAT Signaling and Epigenetic Regulation. Journal of Molecular Diagnostics. 18(5). 707–718. 13 indexed citations
8.
Sorolla, Anabel, Michael R. Tallack, Harald Oey, et al.. (2014). Identification of novel hypomorphic and null mutations in Klf1 derived from a genetic screen for modifiers of α-globin transgene variegation. Genomics. 105(2). 116–122. 12 indexed citations
9.
Perkins, Andrew C., et al.. (2014). KLF1 Null Neonates Display Hydrops Fetalis and a Deranged Erythroid Transcriptome. Blood. 124(21). 2700–2700. 2 indexed citations
10.
Tallack, Michael R. & Andrew C. Perkins. (2013). Three fingers on the switch. Current Opinion in Hematology. 20(3). 193–200. 53 indexed citations
11.
Tallack, Michael R., Graham Magor, Benjamin Dartigues, et al.. (2012). Novel roles for KLF1 in erythropoiesis revealed by mRNA-seq. Genome Research. 22(12). 2385–2398. 81 indexed citations
12.
Sun, Lei, Zhihua Zhang, Timothy L. Bailey, et al.. (2012). Prediction of novel long non-coding RNAs based on RNA-Seq data of mouse Klf1 knockout study. BMC Bioinformatics. 13(1). 331–331. 106 indexed citations
13.
Tallack, Michael R. & Andrew C. Perkins. (2010). KLF1 directly coordinates almost all aspects of terminal erythroid differentiation. IUBMB Life. 62(12). 886–890. 61 indexed citations
14.
Tallack, Michael R., Tom Whitington, Wai Shan Yuen, et al.. (2010). A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells. Genome Research. 20(8). 1052–1063. 175 indexed citations
15.
Tallack, Michael R., Janelle R. Keys, Patrick O. Humbert, & Andrew C. Perkins. (2009). EKLF/KLF1 Controls Cell Cycle Entry via Direct Regulation of E2f2. Journal of Biological Chemistry. 284(31). 20966–20974. 63 indexed citations
16.
Tallack, Michael R. & Andrew C. Perkins. (2009). Megakaryocyte-erythroid lineage promiscuity in EKLF null mouse blood. Haematologica. 95(1). 144–147. 35 indexed citations
17.
Keys, Janelle R., Michael R. Tallack, Ye Zhan, et al.. (2008). A mechanism for Ikaros regulation of human globin gene switching. British Journal of Haematology. 141(3). 398–406. 35 indexed citations
18.
Tallack, Michael R., Janelle R. Keys, & Andrew C. Perkins. (2007). Erythroid Kruppel-like Factor Regulates the G1 Cyclin Dependent Kinase Inhibitor p18INK4c. Journal of Molecular Biology. 369(2). 313–321. 35 indexed citations
19.
Funnell, Alister P. W., Chris Maloney, Lucinda J. Thompson, et al.. (2007). Erythroid Krüppel-Like Factor Directly Activates the Basic Krüppel-Like Factor Gene in Erythroid Cells. Molecular and Cellular Biology. 27(7). 2777–2790. 73 indexed citations
20.
Keys, Janelle R., et al.. (2006). Genomic organisation and regulation of murine alpha haemoglobin stabilising protein by erythroid Kruppel‐like factor. British Journal of Haematology. 136(1). 150–157. 25 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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